首页> 外国专利> Namp;alpha;-2-(4-NITROPHENYLSULFONYL)-ETHOXYCARBONYL-AMINO ACIDS AS Namp;alpha;-PROTECTED AMINO ACIDS FOR SOLID PHASE SYNTHESIS OF PEPTIDES

Namp;alpha;-2-(4-NITROPHENYLSULFONYL)-ETHOXYCARBONYL-AMINO ACIDS AS Namp;alpha;-PROTECTED AMINO ACIDS FOR SOLID PHASE SYNTHESIS OF PEPTIDES

机译:N α -2-(4-硝基苯磺酰基)-乙氧基羰基-酰胺酸作为N α保护的氨基酸,用于固相合成肽

摘要

FIELD:biochemistry,aminoacids,peptides.SUBSTANCE:product:Nα-2-(4-nitrophenylsulfonyl)-ethoxycarbonyl-amino acids: 4-NO2-C6H4-S(O)2-CH2-CH2-O-C(O)-NR1-CHR2-COOH where: R1 - hydrogen; R2 - hydrogen, methyl, isopropyl, methylpropyl, tert.-butoxymethyl, 1-tert.-butoxyethyl, 2-methylthioethyl, benzyl, carboxamidoalkyl, tert.-butoxycarbonylalkyl, or they form together propylene radical. Yield is up to 86%. Reagent 1: the corresponding amino acid. Reagent 2: 2-(4-nitrophenylsulfonyl)-ethylchloroformate. Reaction conditions: aqueous-organic solvent, in the presence of base, at 0-40 C. Synthesized compounds were used as Nα-protected amino acids for solid phase synthesis of peptides. EFFECT: improved method of synthesis, increased yield. 2 tbl
机译:领域:生化,氨基酸,肽。物质:产物:N α -2-(4-硝基苯基磺酰基)-乙氧基羰基-氨基酸:4-NO 2 -C 6 H 4 -S(O) 2 -CH 2 -CH 2 -OC (O)-NR 1 -CHR 2 -COOH其中:R 1 -氢; R 2 -氢,甲基,异丙基,甲基丙基,叔丁氧基甲基,1-叔丁氧基乙基,2-甲基硫乙基,苄基,羧酰胺基烷基,叔丁氧基羰基烷基,或它们一起形成丙烯基。产率高达86%。试剂1:相应的氨基酸。试剂2:2-(4-硝基苯基磺酰基)-乙基氯甲酸酯。反应条件:在碱存在下,在0-40℃下,在水性有机溶剂中。合成的化合物用作N α保护的氨基酸,用于肽的固相合成。效果:改进了合成方法,提高了收率。 2汤匙

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